36C25925Q0074 0001.docx

36C25925Q0074 0001 36C25925Q0074 0001 Amendment hereby incorporates the CPRR per station tests spreadsheet, updated statement of work, and adjusted line-item totals. Deadline for quotes to be submitted has been extended until 01/06/2025 no later than 10:00 MST.

5. PROJECT NUMBER (if applicable)

CODE

7. ADMINISTERED BY

2. AMENDMENT/MODIFICATION NUMBER

CODE

6. ISSUED BY

8. NAME AND ADDRESS OF CONTRACTOR

4. REQUISITION/PURCHASE REQ. NUMBER

3. EFFECTIVE DATE

9A. AMENDMENT OF SOLICITATION NUMBER

9B. DATED

PAGE OF PAGES

10A. MODIFICATION OF CONTRACT/ORDER NUMBER

10B. DATED

BPA NO.

1. CONTRACT ID CODE

FACILITY CODE

CODE

Offers must acknowledge receipt of this amendment prior to the hour and date specified in the solicitation or as amended, by one of the following methods:

The above numbered solicitation is amended as set forth in Item 14. The hour and date specified for receipt of Offers

E. IMPORTANT:

is extended,

(a) By completing Items 8 and 15, and returning __________ copies of the amendment; (b) By acknowledging receipt of this amendment on each copy of the offer submitted; or (c) By separate letter or electronic communication which includes a reference to the solicitation and amendment numbers. FAILURE OF YOUR ACKNOWLEDGMENT TO BE RECEIVED AT THE PLACE DESIGNATED FOR THE RECEIPT OF OFFERS PRIOR TO THE HOUR AND DATE SPECIFIED MAY is not extended.

12. ACCOUNTING AND APPROPRIATION DATA

(REV. 11/2016)

is required to sign this document and return ___________ copies to the issuing office.

is not, A. THIS CHANGE ORDER IS ISSUED PURSUANT TO: (Specify authority) THE CHANGES SET FORTH IN ITEM 14 ARE MADE IN THE CONTRACT ORDER NO. IN ITEM 10A.

15C. DATE SIGNED

B. THE ABOVE NUMBERED CONTRACT/ORDER IS MODIFIED TO REFLECT THE ADMINISTRATIVE CHANGES SET FORTH IN ITEM 14, PURSUANT TO THE AUTHORITY OF FAR 43.103(b).

RESULT IN REJECTION OF YOUR OFFER. If by virtue of this amendment you desire to change an offer already submitted, such change may be made by letter or electronic communication, provided each letter or electronic communication makes reference to the solicitation and this amendment, and is received prior to the opening hour and date specified.

C. THIS SUPPLEMENTAL AGREEMENT IS ENTERED INTO PURSUANT TO AUTHORITY OF:

D. OTHER

Contractor

16C. DATE SIGNED

14. DESCRIPTION OF AMENDMENT/MODIFICATION

16B. UNITED STATES OF AMERICA

Except as provided herein, all terms and conditions of the document referenced in Item 9A or 10A, as heretofore changed, remains unchanged and in full force and effect.

15A. NAME AND TITLE OF SIGNER

16A. NAME AND TITLE OF CONTRACTING OFFICER

15B. CONTRACTOR/OFFEROR

STANDARD FORM 30

PREVIOUS EDITION NOT USABLE

Prescribed by GSA - FAR (48 CFR) 53.243 (Type or print) (Type or print) (Organized by UCF section headings, including solicitation/contract subject matter where feasible.)

(Number, street, county, State and ZIP Code) (If other than Item 6) (Specify type of modification and authority) (such as changes in paying office, appropriation date, etc.)

(If required)

(SEE ITEM 11)

(SEE ITEM 13)

(X)

CHECK

ONE

13. THIS ITEM APPLIES ONLY TO MODIFICATIONS OF CONTRACTS/ORDERS,

IT MODIFIES THE CONTRACT/ORDER NO. AS DESCRIBED IN ITEM 14.

11. THIS ITEM ONLY APPLIES TO AMENDMENTS OF SOLICITATIONS

AMENDMENT OF SOLICITATION/MODIFICATION OF CONTRACT

(Signature of person authorized to sign) (Signature of Contracting Officer) 12-11-2024

36C259-24-AP-0474

36C259 Department of Veterans Affairs Network Contracting Office

NCO 19

6162 South Willow Drive, Suite 300 Greenwood Village

CO

80111 36C259 Department of Veterans Affairs Network Contracting Office

NCO 19

6162 South Willow Drive, Suite 300 Greenwood Village

CO

80111 To all Offerors/Bidders

36C25925Q0074 11-27-2024

X X X ** HOUR & DATE for Receipt of Offers is EXTENDED to: 01-06-2025 10:00 MST See CONTINUATION Page X

AMENDMENT 0001 HEREBY AMENDS SOLICITATION 36C25925Q0074 AS FOLLOWS:

A. VISN Coag CPRR PER STATION SPREADSHEET HAS BEEN INCORPORATED INTO SECTION D.

B. STATEMENT OF WORK HAS BEEN AMENDED TO ADD ADDITIONAL TESTS TO SPECIFIC STATIONS LISTED UNDER "SPECIAL REQUIREMENTS."

C. LINE ITEM QUANTITIES HAVE BEEN ADJUSTED TO REFLECT CORRECT QUANTITIES REQUIRED FOR CONTRACT PERFORMANCE.

D. DEADLINE FOR QUOTES TO BE SUBMITTED HAS BEEN EXTENDED UNTIL 01/06/2025, NO LATER THAN 10:00 MOUNTAIN STANDARD TIME.

E. ALL OTHER TERMS AND CONDITIONS OF THIS SOLICITATION REMAIN UNCHANGED.

LINDSEY ZWAAGSTRA

CONTRACTING OFFICER

VA-VHA-RPOW-2025-0014

CONTINUATION PAGE

STATEMENT OF WORK – VISN COAGULATION ANALYZER

SCOPE:

1. Contractor shall provide all equipment, reagents, standards, controls, supplies, consumable/disposable items, parts, accessories, and any other item required for the proper operation of its Contractor owned coagulation equipment necessary for the generation of a patient Coagulation Cost Per Reportable Result (CPRR).

2. A services component will also be provided for maintenance, repairs, upgrades, trainings, and quality control. Equipment, supplies, and services shall be required for a 5-year ordering period, blanket purchase agreement.

3. Individual facility specific requirements for each location are specified under Special Requirements.

DEFINITIONS:

1. Cost Per Reportable Result (CPRR): The per reportable result price shall include costs covering:

(a) Equipment use;

(b) All reagents, standards, controls, supplies, consumable/disposable items, parts, probes, sampling needles, UPS uninterruptible power supplies, printers, accessories, and any other item required for the proper operation of the Contractor’s equipment and necessary for the generation of a patient reportable result. This does not include those items approved for exclusion by the government such as printer paper, labels etc. This per patient reportable result price shall also encompass all costs associated with dilution, repeat and confirmatory testing required to produce a single patient reportable result. It will also include the material to perform as well as all other costs associated with quality control, calibration and correlation study testing that is prescribed by the Clinical and Laboratory Standards Institute (CLSI);

(c) All necessary maintenance to keep the equipment in good operating condition (This element includes both preventive maintenance and emergency repairs) and;

(d) Training for Government personnel. Contractors are required to provide delivery, installation, and removal of equipment at no additional charge.

GENERAL REQUIREMENTS:

1. Offered models of clinical laboratory coagulation analyzers shall be capable of producing accurate and reproducible results on biological and other specimens by established in vitro diagnostic methods.

2. Model shall provide accurate test assay results for samples up to the manufacturer's defined maximum tests per hour without excessive malfunctions, breakdowns, or service calls.

3. Offered equipment shall be new equipment. Remanufactured and discontinued models will not be accepted.

4. The awarded Contractor shall provide all upgrades and updates to the equipment hardware and operating system software at no additional cost to the Government. These enhancements shall be delivered and installed at the medical facility within 60 days of issuance to the commercial market.

5. VA Office of Information Technology security regulations require Windows based operating systems be Windows 10 or Higher and must be met.

6. The models being offered will be in current production as of the date this offer is submitted. For purposes of this solicitation, “current production” shall mean that the coagulation analyzer model is being manufactured as new equipment. Discontinued models that are only being made available as remanufactured equipment are not acceptable.

7. Contractor offered equipment shall perform satisfactorily at any laboratory temperature between 50- and 90-degrees Fahrenheit with relative humidity between 15 and 85 percent.

8. Contractors offered coagulation system shall conform to existing space and structural parameters in terms of delivery, installation, and lab space. (i.e. equipment size, weight, packaged size for delivery, electrical/voltage).

9. Contractor coagulation system shall be capable of performing the following Clinical Coagulation Assays:

· Prothrombin Time (PT)

· Partial Thromboplastin Time (PTT)

· Fibrinogen (FBG)

· Thrombin Time (TT)

· D-dimer

· Heparin Assay- anti-factor Xa

· Anti-thrombin activity

· Anti-thrombin antigen

· Protein C Activity

· Protein S Activity

· Protein S Free antigen

· Activated Protein C Resistance

· Lupus Anticoagulant testing:

· Factor Assays (II through XII)

· Von Willebrand Antigen

· Von Willebrand Activity

· HIT heparin induced thrombocytopenia

10. Equipment configuration: Contractor owned coagulation systems shall meet the following global criteria for Lab Services:

· Provide broad test menu, with reliable methodologies.

· Ability to perform Heparin anti-Xa and D-dimer assays. (D-dimer should be high sensitivity.)

· Provide both Bar-code operation mode and manual operation mode for samples (operational for reagents and controls).

· Provide Bi-directional interface for Data Innovations with VISTA.

· Provide Bi-directional interface compatible with current system to include all software and hardware to complete movement of data from instrument into Lab Information System and ability to easily re-transmit test result data to host computer.

· Contractor shall be responsible for providing users with lantronix box and adapters, cards, cables, and all required software.

· Accommodate user-defined tests.

· Provide QC (Quality Control) material within the contract.

· Provide Lot Number coordination of reagents and QC materials within the VISN.

· Provide QC inter-laboratory comparison program within the contract.

· Provide assay procedures in CLSI format and on CD-ROM or via Internet (secured).

· Provide Operator's Manual (hard copy or electronic).

· Ability to easily re-transmit test results to host computer.

· Provide on-board Reagent Inventory with the ability to track on board reagent inventory levels including an alert when consumables and supplies are insufficient to process requested tests.

· Have cap piercer, so no uncapping of specimens is necessary.

· Ability to analyze small volume samples.

· Easily understood and performed maintenance procedures. Maintenance procedures should take less than one hour for each daily, weekly, or monthly requirements, this means total time, not hands-on tech time.

· Contractor shall replace and maintain UPS unit and batteries per instrument per site.

· Provide long shelf-life for Reagents and controls, including on-board stability. One year for PT and PTT assays and 6 months for D-Dimer and Fibrinogen.

· Contractor will provide SDS and Waste stream disposal requirements for all reagents.

· Contractor shall provide printer capable of producing patient and QC reports. Contractor to replace if needed.

· PT Reagent ISI near 1.0

· CAP Piercing and Auto Sampling with 15-30 slots for tubes.

· Provide STAT and random-access capabilities for all testing and auto-rerun for longer running tests.

· Provide QC material with 2-3 distinct levels of controls for PT and PTT.

· Contractor performs validation, linearity, precision correlation and normal range studies at Contractor’s expense prior to going live.

· Uninterrupted access to reagent and cuvette loading.

· Detection and alert of sample integrity including hemolysis, icterus and lipemia. Detection and alert of underfilled samples.

· Automatic quality control and maintenance at set times.

· High volume, ready to use reagents with extended on-board stability.

· Ability of software to store multiple curves per analyte.

· Ability to view individual specimen curves to determine specimen acceptability.

· Peer group for CAP Proficiency surveys (equipment/reagent system) shall contain at least 50 labs.

· Analyzer shall be capable of performing PTs, PTTs and D-dimers, at a minimum – with ability to add more assays.

· Sample primary tubes and short samples/cup sampling with level detection for adequate sampling.

· Provide Linearity samples covering the analytical measuring range of the instrument required every 6 months by CLIA 88.

· Provide PT and PTT Lot to Lot studies as required by CLIA 88.

· Level sense for adequate sample detection.

· Contain a user-friendly QC program with peer group comparisons and data that is submitted electronically monthly.

· Ability to manually order tests.

· Random access test performance capability.

· Reagent monitoring (by instrument).

· Provide sequestering of reagent and QC lots.

11. Pricing: Contractor shall provide pricing for each test in accordance with the CPRR definition stated above, that can be performed on the quoted equipment. The CPRR shall include all costs for:

· Equipment uses.

· All consumables, reagents, standards, controls, and supplies.

· All necessary maintenance to keep equipment in manufacturer's operating condition by providing comprehensive maintenance to include both preventive maintenance and emergency repairs.

· Training for facility personnel operating equipment.

· The technical description of the products should contain information such as actual number of tests performed per kit, including controls, calibrations, CAP surveys, patient test, etc. This information shall include, at a minimum, the expected out-dating and open vial stability of the kits and controls, frequency of calibrations, and how long calibration curves are stable, etc.

· The Contractor is required to provide delivery, installation, final placement, and removal of equipment and packaging materials at no additional charge.

· All consumable supplies (reagents, standards, control, disposables, etc.) required for the proper operation to the Contractor’s equipment and necessary to perform tests on the equipment provided shall be included and shall be furnished by the Contractor for each coagulation analyzer.

· In the event the consumables are found to be defective and unsuitable for use with the Contractor's equipment, or the Contractor has failed to comply with the requirements for routine supply delivery, the Contractor shall deliver the consumable supplies within a period of twenty-four (24) hours after receipt of the verbal order for priority delivery from the Government activity. If either circumstance has occurred, the Contractor shall deliver to the requesting lab facility, in the most expeditious manner possible, without additional cost to the Government, the necessary consumables in sufficient quantity as required to allow operation of the Contractor's equipment for one week (under normal Government test load volume). If additional requests for emergency supply delivery are required by the Government, they will be honored by the Contractor until the arrival at the Government site of the monthly standing order/routine supplies delivery. Failure to reserve adequate inventory may result in default.

12. Inventory Control of Reagents Supplies and Disposables:

· The Contractor shall provide the Government inventory of reagents, standards, controls, supplies, disposables, and any other material required to properly perform tests on the offered equipment. These items shall be of the highest quality ensuring sensitivity, specificity and tested to assure precision and accuracy. The quality of the products shall be high enough to satisfy proficiency testing standards of the College of American Pathologists (CAP) and The Joint Commission (JC) on accreditation of Health Care Organizations.

· If, for any reason, the Contractor ceases testing of any Coagulation assays, the Contractor must notify the Contract Specialist or Contracting Officer 60 days prior to the change. Until a new solicitation can be issued, or the problem resolved, the Contractor shall be held liable for all costs if performance is ceased, as the lab facility may have to resort to outsourcing the tests in order to continue patient care.

13. Maintenance and Repairs:

· With the exception of the specific maintenance and repair requirements stated herein, which shall have precedence; preventive maintenance, emergency repair, maintenance credit for equipment malfunction, and replacement laboratory equipment shall be performed and provided in accordance with the terms, conditions, and provisions of Contractor's existing Federal Supply Service Contract.

· Emergency repairs shall be performed after initial telephone notification that the equipment is inoperative. The Contractor shall provide the Government with a designated point of contact and telephone number and shall arrange to enable his maintenance representative to receive such notification.

· The Contractor shall be on-site at the affected VA facility to perform emergency repair service within twenty-four (24) hours after receipt of initial telephone notification of a malfunction. Contractor shall provide medical center maintenance coverage 24 hours per day, seven days per week including all Federal holidays, excluding Ernest Childers VA Clinic, Sheridan VA Lab, Fort Sill Lawton, and Billings VA Healthcare Center, which require service Monday – Friday, 08:00 a.m. until 04:30 p.m., excluding Federal holidays.

· Contractor shall provide technical support service to assist in troubleshooting 24 hours per day, seven days per week including Federal holidays.

· For sites that maintain backup instruments for full menu duplication (Salt Lake City, Aurora, Fort Harrison, Grand Junction, Cheyenne, Lawton, Oklahoma City, and Muskogee), all instruments placement by vendor must retain all menu throughput needs.

· In addition to above, the Contractor shall furnish a malfunction incident report to the affected VA facility upon completion of each repair call. The report shall include, as a minimum, the following:

A. date and time notified

B. date and time of arrival

C. serial number, type and model number(s) of equipment

D. time spent for repair

E. description of malfunction and repair

F. proof of repair that includes documentation verifying acceptable performance.

· Should the repair record of any individual piece of laboratory equipment reflect a downtime of 5% or greater of the normal working days in one calendar month, a determination will be made by the designated representative of the Government at the using facility to replace the initial laboratory equipment with new equipment. The responsibility for maintaining the equipment furnished in good condition in accordance with manufacturer’s instructions shall be solely that of the Contractor. Each instrument provided by the Contractor shall maintain an uptime of 95% in each month of the term of the agreement.

· The Contractor shall not leave a service call open. Once repairs have been completed by the Contractor’s maintenance personnel, the service call associated with the repair shall be closed. For each instrument provided the Contractor shall treat each notification for an emergency/repair service call from the Government as a separate and new service call.

14. Training:

· With the exception of the specific training requirements stated herein, which shall have precedence; Contractor shall provide training.

· Provide initial in-depth training for two key operators at the facility and for each individual instrument provided.

· Provide annual training for one VA equipment operator, per each instrument, for each participating medical center at contractor’s facility, if available.

· Provide on-site vendor operator training for all personnel who will run instrument with training provided for all applicable shifts.

15. Vaporware:

· Any proposed equipment and functions which are based on the advent of vaporware shall not be considered. Vaporware is any equipment, systems, components, software, not currently available or pending any type of approval, including FDA, before it can be released to the public. All equipment, software, etc. shall be available at the time offers are submitted.

16. Space Availability:

· All proposed equipment must fit the existing space at the affected VA site, without the need for renovation work. Small scale re-arrangement of furniture is acceptable. Fitting existing space shall include conforming to the current structural parameters of each lab, in each facility, in terms of delivery, installation and lab space (i.e. equipment size, weight, packaged size for delivery, electrical/voltage).

· A total equipment footprint that when installed in the laboratory shall not impact the functionality/operations of that laboratory.

SPECIAL REQUIREMENTS:

In addition to the general requirements for Coagulation Cost-Per-Reportable Result stated above, the Contractor shall provide equipment and peripherals necessary to meet the specialized configurations described for each of the participating medical facilities. Contractor equipment and systems shall conform to the following parameters for each of the facilities.

1. Station 554 Rocky Mountain Regional VA Medical Center, 1700 North Wheeling Street, Aurora, CO 80045:

The Contractor shall provide two (2) identical analyzers, for which each analyzer shall conform to the following:

· Provide (2) printers and (2) UPS units.

· FDA approved HIT, Heparin Induced Thrombocytopenia, testing.

· HIT testing can be performed by routine coagulation instrumentation.

· Space dimension for each analyzer is 60-inch length and 30-inch width (deep).

· Maximum allowable height from countertop is 65 inches.

· 2 Floor drains available.

· One sink is available.

· No deionized water source.

· 2 immobile power source poles.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), Fibrinogen (FBG), Anti-Thrombin III (ATIII), D-dimer, Protein C Activity, Protein S Free Antigen, Activated Protein C Resistance, Lupus Anticoagulant testing: Dilute Russell Viper Venom Time, Lupus Anticoagulant testing: Lupus Anticoagulant Test, Factor Assays (II through XII), Von Willebrand Activity, Von Willebrand Antigen, Anti-factor Xa, and HIT Heparin Induced Thrombocytopenia.

2. Station 666 Sheridan VA Medical Center, 1898 Fort Road, Sheridan, WY 82801 The Contractor shall provide one (1) analyzer, which shall conform to the following:

· Provide (1) UPS and (1) printer.

· Space dimension for analyzer Total counter space = 33”d x 95”w x 38” h

· Maximum allowable height from countertop is 38 inches.

· There is one sink currently used as a drain for current coagulation analyzer.

· No deionized water source.

· 8 power outlets.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), and D-dimer.

3. Station 436B Billings VA Healthcare Center, 1766 Majestic Lane, Billings, MT 59102:

The Contractor shall provide one (1) analyzer, which shall conform to the following:

· Provide (1) UPS and (1) Printer.

· Space Dimensions for analyzer 74-inch length x 57-inch wide

· Maximum allowable height is 65 inches from countertop.

· No sink or drain near coagulation analyzer.

· No deionized water source.

· 2 power outlets.

· Tests required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), and D-dimer.

4. Station 436FH VA Montana Health Care System, 3717 Veterans Drive, Fort Harrison, MT 59636:

The Contractor shall provide two (2) analyzers (primary and backup), which shall conform to the following:

· Provide (2) UPS and (2) printers.

· Primary Instrument plus backup instrument and all associated CRT/PC units must fit into a linear countertop measurement. Backup instrument shall have automated sample-handling capabilities.

· Space dimensions for analyzers 70 inches in length and 30 inches wide/deep.

· Maximum allowable height is 30 inches from countertop.

· (4) 120Volt outlets are in this location.

· Drain tubes needs to be 10 feet in length in this location.

· The counter can hold up to 300 lbs.

· Tests required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), D-dimer, and Fibrinogen.

5. Station 635 Oklahoma City VA Healthcare System, 921 NE 13th Street, Oklahoma City, Oklahoma 73104 The Contractor shall provide two (2) identical analyzers, for which each analyzer shall conform to the following:

· Provide (2) printers and (2) UPS units.

· Space dimensions for analyzers 144 inches in length and 48 inches wide/deep.

· Maximum allowable height is 65 inches from countertop.

· No drain or sink available for instrument draining.

· De-ionized water source is available, but it is not used for coagulation analyzer.

· 8 power outlets.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), Fibrinogen (FBG), and D-Dimer.

6. Station 635 Lawton/Ft Sill VA Outpatient Clinic, 4303 Pitman Street Fort Sill Oklahoma The Contractor shall provide two (2) analyzers, for which will conform to the following:

· Provide (2) printers and (2) UPS units.

· Space dimensions for analyzers 80 inches length and 30 inches wide/deep.

· Maximum allowable height is 65 inches from countertop.

· 1 drain and 1 sink available.

· No deionized water source.

· 8 power outlets.

· Tests Required: Prothrombin Time (PT).

7. Station 575 Grand Junction VA Medical Center, 2121 North Avenue, Grand Junction, CO 81501:

The Contractor shall provide two (2) analyzers (primary and backup) which shall conform to the following:

· Provide (2) Printers and (2) UPS units.

· Space dimensions for each analyzer-42 inches length and 29 inches width (the countertop is 29 inches deep).

· Maximum allowable height is 32 inches from countertop.

· There are no sinks or drains accessible to the analyzers.

· The analyzers are not connected to a water source.

· 3 wall outlets for a total of 6 per instrument.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), D-dimer, and Anti-Xa.

8. Station 442 Cheyenne VA Medical Center, 2360 E. Pershing "Blvd., Cheyenne, WY 82001:

The Contractor shall provide (2) mirrored analyzers, which shall conform to the following:

· Shall provide various test processing capability - PT, PTT, D-Dimer (High Sensitivity exclusion), Heparin anti factor 10-a, HIT heparin induced thrombocytopenia would be a highly desired test.

· Provide (2) Printers and (2) UPS units.

· Space dimensions for analyzers 16'x2" length x 28.5" wide.

· Maximum allowable height is 65 inches from countertop.

· Drain will be the closest dirty sink.

· There is no deionized water source.

· 7 power outlets.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), D-Dimer, Anti-factor Xa, and HIT Heparin Induced Thrombocytopenia.

9. Station 660 VAMC Salt Lake City, UT 500 Foothill Dr. SLC, UT 84148:

The Contractor shall provide two (2) identical analyzers, for which each analyzer shall conform to the following:

· Provide (2) printers and (2) UPS units.

· Space dimensions for analyzers-two lab owned instrument tables measuring 5’ x 3’ x 3’

· 4 data ports.

· 8” floor drain.

· No deionized water source.

· 6 power outlets.

· Tests Required: Prothrombin Time (PT), Partial Thromboplastin Time (PTT), Fibrinogen (FBG), and D-Dimer,

10. Station 623 Eastern Oklahoma VA Health Care System, 1011 Honor Heights Dr, Muskogee, Ok 74401 The Contractor shall provide two (2) identical analyzers, for which each analyzer shall conform to the following:

· Provide (2) printers and (2) UPS units.

· Space dimensions-2 Tables (30”W x 72”L) (30”W x 84”L)

· Maximum allowable height is 30 inches from countertop.

· No sink or drain next to tables.

· Independent deionized water system used for chemistry analyzers.

· Tests Required: Prothrombin Time (PT), and Partial Thromboplastin Time (PTT).

11. Station 623 Ernest Childers VA Health Care Center, 8921 S. Mingo Rd., Tulsa, OK 74133 The Contractor shall provide one (1) analyzer, for which will conform to the following:

· Provide (1) printer and (1) UPS unit.

· Space dimensions for benchtop coagulation analyzer: 36” L x 24” W x 54” H

· Maximum allowable height is 54” from countertop.

· 1 drain, but no sink available.

· No deionized water source specifically for coagulation.

· 2 power outlets.

· Tests Required: Prothrombin Time (PT), and Partial Thromboplastin Time (PTT).

TRANSITION PERIOD:

1. Upon award of the contract, the transition period for the awarded Contractor to have all Coagulation equipment and peripherals installed at the effected facility shall be 30-60 calendar days after award. During this same period all initial training of VA personnel in the operation and maintenance of said equipment shall also be completed.

2. No later than 60-90 calendar days after installation, the Contractor shall have completed full transition of all services under this agreement to include all correlation studies, validations, etc., and shall have full and sole responsibility for equipment, supplies, and services under the awarded contract.

3. Billing by Contractor starts on the first day of patient testing after all installation, training, and method validations have been completed and accepted in writing by the Contract Specialist (no later than 90-120 calendar days from time of award). At this time, the awarded Contractor shall have completed full transition of all equipment, supplies and services under this agreement and shall have full and sole responsibility for equipment, supplies, and services under the awarded contract.

CONTROL PACKAGES INCLUDED:

1. Contractor shall provide the description/items of control packages/consumables included in Coagulation Cost per Reportable Result here. Need to define No item or part required for operation of machines and system will be listed as a consumable item and require a separate charge to the facility this includes sample needles, tube grabbers, reagent pickup straws, and the like.

A.1 PRICE/COST SCHEDULE

ITEM INFORMATION

436B Billings VA Healthcare Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

Contract Period: Base POP Begin: 02-01-2025 POP End: 01-31-2030 PRINCIPAL NAICS CODE: 334516 - Analytical Laboratory Instrument Manufacturing PRODUCT/SERVICE CODE: 6640 - Laboratory Equipment and Supplies

436FH Fort Harrison VA Montana Health Care System Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

442 Cheyenne VA Medical Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

554 Rocky Mountain Regional VA Medical Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

575 Grand Junction VA Medical Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

623 Eastern Oklahoma VA Health Care System Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

623 Ernest Childers VA Health Care Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

635 Oklahoma City VA Healthcare System Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

635 Lawton/Ft Sill VA Outpatient Clinic Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

660 VAMC Salt Lake City Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

666 Sheridan VA Medical Center Funding CLIN to provide funding for authorized callers to purchase items as needed. This is a not to exceed task order IAW FAR 52.213-3 Notice to Supplier.

POP Begin: 02-01-2025 POP End: 01-31-2030

Prothrombin Time (PT)

POP Begin: 02-01-2025 POP End: 01-31-2030

Partial Thromboplastin Time (PTT)

POP Begin: 02-01-2025 POP End: 01-31-2030

Fibrinogen (FBG)

POP Begin: 02-01-2025 POP End: 01-31-2030

Thrombin Time (TT)

POP Begin: 02-01-2025 POP End: 01-31-2030

Anti-Thrombin III (ATIII)

POP Begin: 02-01-2025 POP End: 01-31-2030

D-Dimer

POP Begin: 02-01-2025 POP End: 01-31-2030

Heparin Assay (covered under Anti-Factor XA)

POP Begin: 02-01-2025 POP End: 01-31-2030

Anti-Thrombin Activity (Covered under Anti-Thrombin III)

POP Begin: 02-01-2025 POP End: 01-31-2030

Anti-Thrombin Antigen

POP Begin: 02-01-2025 POP End: 01-31-2030

Protein C Activity

POP Begin: 02-01-2025 POP End: 01-31-2030

Protein S Activity

POP Begin: 02-01-2025 POP End: 01-31-2030

Protein S Free Antigen

POP Begin: 02-01-2025 POP End: 01-31-2030

Activated Protein C Resistance

POP Begin: 02-01-2025 POP End: 01-31-2030

Lupus Anticoagulant testing: Dilute Russell Viper Venom Time

POP Begin: 02-01-2025 POP End: 01-31-2030

Lupus Anticoagulant testing: Hexagonal phase phospholipid

POP Begin: 02-01-2025 POP End: 01-31-2030

Von Willebrand Activity

POP Begin: 02-01-2025 POP End: 01-31-2030

Von Willebrand Antigen

POP Begin: 02-01-2025 POP End: 01-31-2030

Anti-factor Xa

POP Begin: 02-01-2025 POP End: 01-31-2030

HIT Heparin Induced Thrombocytopenia

POP Begin: 02-01-2025 POP End: 01-31-2030

Factor Assay VIII

POP Begin: 02-01-2025 POP End: 01-31-2030

Factor Assay IX

POP Begin: 02-01-2025 POP End: 01-31-2030

Factor X Assay

POP Begin: 02-01-2025 POP End: 01-31-2030

Page 1 of

SECTION D - CONTRACT DOCUMENTS, EXHIBITS, OR ATTACHMENTS

VISN Coag CPRR Per Station See attached document: VISN Coag CPRR Per Station FINAL.

Page 1 of